Kinetics investigation of the synthesis reaction of 2,3-dihydroquinazolin-4(1H)-ones in the presence of acetic acid as a catalyst
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Abstract:
Acetic acid has been applied as an efficient catalyst and a green solvent for the two–component condensation reaction consisting of benzaldehyde, 2-amino-benzamide. The advantages of this protocol was excellent yield, short reaction time, mild reaction conditions, higher availability, low costs, more environmentally friendly, lack of need for column chromatography and simple work-up procedure. In addition, based on the spectral data, the partial order with respect to each reactant was one. Furthermore, useful information regarding the mechanism of the reaction was obtained from studies of the effect of solvent, concentration and catalyst on the rate of the reaction. The results showed that the first step of the mechanism was a rate-determining step. In the studied temperature range, the second order rate constant (lnk1, lnk1/T) depended on reciprocal temperature was in good agreement with the Arrhenius and Eyring equations. These data provided the suitable plots for calculating the activation energy (Ea = 52.80 kJmol-1) and the related kinetic parameters (ΔG‡ = 63.74 kJmol-1, ΔS‡ = -54.22 Jmol-1 and ΔH‡ = 50.28 kJmol-1) of the reaction.
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kinetics investigation of the synthesis reaction of 2,3-dihydroquinazolin-4(1h)-ones in the presence of acetic acid as a catalyst
acetic acid has been applied as an efficient catalyst and a green solvent for the two–component condensation reaction consisting of benzaldehyde, 2-amino-benzamide. the advantages of this protocol was excellent yield, short reaction time, mild reaction conditions, higher availability, low costs, more environmentally friendly, lack of need for column chromatography and simple work-up procedure. ...
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comparison of catalytic activity of heteropoly compounds in the synthesis of bis(indolyl)alkanes.
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Journal title
volume 4 issue 4
pages 241- 246
publication date 2014-12-01
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